Signaling by intrathymic cytokines, not T cell antigen receptors, specifies CD8 lineage choice and promotes the differentiation of cytotoxic-lineage T cells

JH Park, S Adoro, T Guinter, B Erman, AS Alag… - Nature …, 2010 - nature.com
JH Park, S Adoro, T Guinter, B Erman, AS Alag, M Catalfamo, MY Kimura, Y Cui, PJ Lucas…
Nature immunology, 2010nature.com
Abstract Immature CD4+ CD8+ (double-positive (DP)) thymocytes are signaled via T cell
antigen receptors (TCRs) to undergo positive selection and become responsive to
intrathymic cytokines such as interleukin 7 (IL-7). We report here that cytokine signaling is
required for positively selected thymocytes to express the transcription factor Runx3, specify
CD8 lineage choice and differentiate into cytotoxic-lineage T cells. In DP thymocytes
genetically engineered to be cytokine responsive, IL-7 signaling induced TCR-unsignaled …
Abstract
Immature CD4+CD8+ (double-positive (DP)) thymocytes are signaled via T cell antigen receptors (TCRs) to undergo positive selection and become responsive to intrathymic cytokines such as interleukin 7 (IL-7). We report here that cytokine signaling is required for positively selected thymocytes to express the transcription factor Runx3, specify CD8 lineage choice and differentiate into cytotoxic-lineage T cells. In DP thymocytes genetically engineered to be cytokine responsive, IL-7 signaling induced TCR-unsignaled DP thymocytes to express Runx3 and to differentiate into mature CD8+ T cells, completely circumventing positive selection. We conclude that TCR-mediated positive selection converts DP cells into cytokine-responsive thymocytes, but it is subsequent signaling by intrathymic cytokines that specifies CD8 lineage choice and promotes differentiation into cytotoxic-lineage T cells.
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